A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150239



Internal ID15879149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77792218..77821639hg38UCSC Ensembl
Innerchr2:78019344..78048765hg19UCSC Ensembl
Innerchr2:77872852..77902273hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3829422
hg1929422
hg1829422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582267
Supporting Variants
SamplesHGDP01318
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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